ENST00000492653.6:c.*239T>A
|
ENSP00000515192.1:n.*239T>A
|
|
ENST00000703133.1:c.*1189T>A
|
ENSP00000515188.1:n.*1189T>A
|
|
ENST00000703136.1:c.*573T>A
|
ENSP00000515190.1:n.*573T>A
|
|
ENST00000374839.8:c.615T>A
MANE Select
|
ENSP00000363972.3:p.Leu205=
|
|
ENST00000337990.2:c.546T>A
|
ENSP00000338650.2:p.Leu182=
|
|
ENST00000374839.7:c.615T>A
|
ENSP00000363972.3:p.Leu205=
|
|
ENST00000447788.6:c.452T>A
|
ENSP00000399126.2:p.Phe151Tyr
|
|
ENST00000488406.1:n.135T>A
|
|
|
ENST00000488608.5:n.2792T>A
|
|
|
ENST00000488831.5:n.603T>A
|
|
|
ENST00000492653.5:n.743T>A
|
|
|
NM_001178032.2:c.546T>A
|
NP_001171503.1:p.Leu182=
|
|
NM_001178033.2:c.452T>A
|
NP_001171504.1:p.Phe151Tyr
|
|
NM_001243804.1:c.546T>A
|
NP_001230733.1:p.Leu182=
|
|
NM_018684.3:c.615T>A
|
NP_061154.1:p.Leu205=
|
|
NR_045044.1:n.1026T>A
|
|
|
NM_018684.4:c.615T>A
MANE Select
|
NP_061154.1:p.Leu205=
|
|
NM_001178032.3:c.546T>A
|
NP_001171503.1:p.Leu182=
|
|
NM_001243804.2:c.546T>A
|
NP_001230733.1:p.Leu182=
|
|
NR_045044.2:n.943T>A
|
|
|
NM_001178033.3:c.452T>A
|
NP_001171504.1:p.Phe151Tyr
|
|